Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Patrick L, Heilman"'
Autor:
Raphael A. Malbrue, Lori Mattox, Stephen J. Kolb, Charlotte J. Sumner, Jessica Russo, Kelly A. Rich, Megan G. Pino, Patrick L. Heilman, Christopher G. Wier, Lingling Kong, Elizabeth Keckley, Anthony B. Reynolds, Amy Knapp, Catalin S. Buhimschi
Publikováno v:
Gene Ther
Numerous pediatric neurogenetic diseases may be optimally treated by in utero gene therapy (IUGT); but advancing such treatments requires animal models that recapitulate developmental physiology relevant to humans. One disease that could benefit from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31b849da8aafad37f4d434196f7e736d
https://europepmc.org/articles/PMC10216882/
https://europepmc.org/articles/PMC10216882/
Autor:
Patrick L. Heilman, Alexander E. Crum, Marilly Palettas, Stephen J. Kolb, Christopher G. Wier, David Kline, Chitra C. Iyer, Deepti Chugh, W. David Arnold, Anthony B. Reynolds
Publikováno v:
Muscle & Nerve. 59:254-262
Introduction Electrophysiological measurements are used in longitudinal clinical studies to provide insight into the progression of amyotrophic lateral sclerosis (ALS) and the relationship between muscle weakness and motor unit (MU) degeneration. Her
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fea4322d522ce7f85a4ec1525e0ef34f
https://doi.org/10.1002/mus.26365
https://doi.org/10.1002/mus.26365
Autor:
Kathrin Meyer, Brian K. Kaspar, SungWon Song, Patrick L. Heilman, Carlos Henrique Miranda, Christopher G. Wier, Amy Knapp, Stephen J. Kolb, Amit K. Srivastava
Publikováno v:
Experimental Neurology. 297:101-109
Heat shock protein beta-1 (HSPB1), is a ubiquitously expressed, multifunctional protein chaperone. Mutations in HSPB1 result in the development of a late-onset, distal hereditary motor neuropathy type II (dHMN) and axonal Charcot-Marie Tooth disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78e679b77b6a093139b9f52efaa5ec3d
https://doi.org/10.1016/j.expneurol.2017.08.002
https://doi.org/10.1016/j.expneurol.2017.08.002
Autor:
Christopher G, Wier, Alexander E, Crum, Anthony B, Reynolds, Chitra C, Iyer, Deepti, Chugh, Marilly S, Palettas, Patrick L, Heilman, David M, Kline, W David, Arnold, Stephen J, Kolb
Publikováno v:
Musclenerve. 59(2)
Electrophysiological measurements are used in longitudinal clinical studies to provide insight into the progression of amyotrophic lateral sclerosis (ALS) and the relationship between muscle weakness and motor unit (MU) degeneration. Here, we used a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::98f966f37edb72f951bff8af6b04d2fa
https://pubmed.ncbi.nlm.nih.gov/30461038
https://pubmed.ncbi.nlm.nih.gov/30461038